Angiofibromas in multiple endocrine neoplasia type 1

Neelam Vashi, Raegan Hunt, Max Fischer, Shane Meehan, Miriam Keltz Pomeranz

Research output: Contribution to journalArticle

Abstract

Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.

Original languageEnglish (US)
Pages (from-to)20
Number of pages1
JournalDermatology Online Journal
Volume18
Issue number12
StatePublished - Dec 2012
Externally publishedYes

Fingerprint

Angiofibroma
Multiple Endocrine Neoplasia Type 1
Lipoma
Tumor Biomarkers
Neoplasms
Skin

ASJC Scopus subject areas

  • Dermatology

Cite this

Vashi, N., Hunt, R., Fischer, M., Meehan, S., & Pomeranz, M. K. (2012). Angiofibromas in multiple endocrine neoplasia type 1. Dermatology Online Journal, 18(12), 20.

Angiofibromas in multiple endocrine neoplasia type 1. / Vashi, Neelam; Hunt, Raegan; Fischer, Max; Meehan, Shane; Pomeranz, Miriam Keltz.

In: Dermatology Online Journal, Vol. 18, No. 12, 12.2012, p. 20.

Research output: Contribution to journalArticle

Vashi, N, Hunt, R, Fischer, M, Meehan, S & Pomeranz, MK 2012, 'Angiofibromas in multiple endocrine neoplasia type 1', Dermatology Online Journal, vol. 18, no. 12, pp. 20.
Vashi N, Hunt R, Fischer M, Meehan S, Pomeranz MK. Angiofibromas in multiple endocrine neoplasia type 1. Dermatology Online Journal. 2012 Dec;18(12):20.
Vashi, Neelam ; Hunt, Raegan ; Fischer, Max ; Meehan, Shane ; Pomeranz, Miriam Keltz. / Angiofibromas in multiple endocrine neoplasia type 1. In: Dermatology Online Journal. 2012 ; Vol. 18, No. 12. pp. 20.
@article{691e614da0f74878b05041dd71a79de3,
title = "Angiofibromas in multiple endocrine neoplasia type 1",
abstract = "Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.",
author = "Neelam Vashi and Raegan Hunt and Max Fischer and Shane Meehan and Pomeranz, {Miriam Keltz}",
year = "2012",
month = "12",
language = "English (US)",
volume = "18",
pages = "20",
journal = "Dermatology Online Journal",
issn = "1087-2108",
publisher = "Department of Dermatology UC Davis",
number = "12",

}

TY - JOUR

T1 - Angiofibromas in multiple endocrine neoplasia type 1

AU - Vashi, Neelam

AU - Hunt, Raegan

AU - Fischer, Max

AU - Meehan, Shane

AU - Pomeranz, Miriam Keltz

PY - 2012/12

Y1 - 2012/12

N2 - Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.

AB - Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.

UR - http://www.scopus.com/inward/record.url?scp=84871527463&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84871527463&partnerID=8YFLogxK

M3 - Article

VL - 18

SP - 20

JO - Dermatology Online Journal

JF - Dermatology Online Journal

SN - 1087-2108

IS - 12

ER -